Canonical Allele Identifier: CA1619077590
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269293T= , CM000668.2:g.31269293T= GRCh38
NC_000006.11:g.31237070T= , CM000668.1:g.31237070T= GRCh37
NC_000006.10:g.31345049T= NCBI36
NG_029422.2:g.7839A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1096+45A= MANE Select ENSP00000365402.5:n.1096+45A=
ENST00000376228.9:c.1096+45A= ENSP00000365402.5:n.1096+45A=
ENST00000376237.8:c.*683+45A= ENSP00000365412.4:n.*683+45A=
ENST00000383329.7:c.1114+45A= ENSP00000372819.3:n.1114+45A=
ENST00000466892.5:n.329+45A=
ENST00000470363.5:n.854+45A=
ENST00000487245.5:n.1455+45A=
NM_002117.5:c.1096+45A= NP_002108.4:n.1096+45A=
NM_002117.6:c.1096+45A= MANE Select NP_002108.4:n.1096+45A=
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